Taiwan FDA registration 5e524144c882b901d21d80a7bacc1538
Badi Tieke High Sensitivity C-Reactive Protein Quality Tube
TW: 巴迪鐵克高靈敏性 C 反應蛋白品管液
Taiwan·Risk Class 2·Boditech Med Inc.·Registered Mar 04, 2024 – Mar 04, 2029ActiveRegistration details
- Analysis ID
- 5e524144c882b901d21d80a7bacc1538
- Customs Code
- DHA05603706508
Company information
- Manufacturer
- Boditech Med Inc.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MEDRICH INSTRUMENT CO., LTD.
Product details
- Intended Use
- This product is used for quality control of highly sensitive C-reactive protein assays manufactured and supplied by Boditech.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 04, 2024
- Expiry Date
- Mar 04, 2029
About this record
Access comprehensive regulatory information for Badi Tieke High Sensitivity C-Reactive Protein Quality Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e524144c882b901d21d80a7bacc1538 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices